C–H alkenylation/cyclization and sulfamidation of 2-phenylisatogens using N-oxide as a directing group-Reference-Cited by-同舟云学术

C–H alkenylation/cyclization and sulfamidation of 2-phenylisatogens using N-oxide as a directing group

Published:2019 Issue:71 Volume:55 Page:10623-10626
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Guo Lingmei¹²³⁴⁵,Tang Baolan¹²³⁴⁵,Nie Ruifang¹²³⁴⁵,Liu Yanzhao¹²³⁴⁵,Lv Shan¹²³⁴⁵,Wang Huijing⁶⁷⁸⁹,Guo Li¹²³⁴⁵,Hai Li¹²³⁴⁵^ORCID,Wu Yong¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Drug Targeting and Drug Delivery System of Education Ministry

2. Department of Medicinal Chemistry

3. West China School of Pharmacy

4. Sichuan University

5. Chengdu

6. Skaggs School of Pharmacy and Pharmaceutical Sciences

7. University of California San Diego

8. La Jolla

9. USA

Abstract

Ru(ii)-Catalyzed C–H alkenylation/cyclization and Ir(iii)-catalyzed C–H sulfamidation provided indol-3-one derivatives and sulfamidated 2-phenylisatogens respectively, with good yields and excellent functional group tolerance.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC05719F

Reference76 articles.

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4. Cobalt(iii)-catalyzed annulation of esters and alkynes: a facile route to indenones

5. Rhodium-Catalyzed Direct Ortho C–H Arylation Using Ketone as Directing Group with Boron Reagent

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